ENANTIOSELECTIVE RECOGNITION OF THE PHENACETYL MOIETY IN THE PEN-G ACYLASE CATALYZED-HYDROLYSIS OF PHENYLACETATE ESTERS

Authors
FUGANTI C ROSELL CM SERVI S TAGLIANI A TERRENI M
Citation
C. Fuganti et al., ENANTIOSELECTIVE RECOGNITION OF THE PHENACETYL MOIETY IN THE PEN-G ACYLASE CATALYZED-HYDROLYSIS OF PHENYLACETATE ESTERS, Tetrahedron : asymmetry, 3(3), 1992, pp. 383-386
Citations number
18
Categorie Soggetti
Chemistry Inorganic & Nuclear","Chemistry Inorganic & Nuclear
Journal title
Tetrahedron : asymmetry → ACNP
ISSN journal
09574166
Volume
3
Issue
3
Year of publication
1992
Pages
383 - 386
Database
ISI
SICI code
0957-4166(1992)3:3<383:EROTPM>2.0.ZU;2-1
Abstract
Penicillin G acylase from E. coli (E.C. 3.5.1.11) immobilized on Euper git C enantioselectively recognises phenyl acetates derivatives allowi ng the preparation of compounds of high ee to be used as side chains i n the preparation of beta-lactam antibiotics.